Results 141 to 150 of about 7,513 (218)

Study of the meiotic segregation of chromosome 7 with a paracentric inversion in spermatosoa of a heterozygous carrier. [PDF]

Vavilovskii Zhurnal Genet Selektsii
Antonova MM, Yurchenko DA, Markova ZG, Shilova NV.   +3 more
europepmc   +1 more source

Non-invasive image study of bone bioerosion in Spanish Civil War lime graves. [PDF]

Sci Rep
Gutiérrez A, Rey-Rodríguez I, Macho-Callejo A, Armentano N, Fernández-Jalvo Y.   +4 more
europepmc   +1 more source

Functional and genomic characterization of polyethylene degrading yeast Meyerozyma carpophila M6.0.2 isolated from marine plastic debris in East Java Indonesia. [PDF]

Sci Rep
Alami NH, Puteri ZR, Esaki T, Sugai Y, Pratama F, Purwasena IA, Aditiawati P.   +6 more
europepmc   +1 more source

Selecting stable rice mutants with linear mixed models (LMM) and stability indexes. [PDF]

Vavilovskii Zhurnal Genet Selektsii
Sharifi P, Ebadi AA, Hallajian MT, Aminpanah H.   +3 more
europepmc   +1 more source

Familial translocation between chromosomes 3 and 10: meiotic segregation, diagnostics and clinical features of chromosomal imbalance. [PDF]

Vavilovskii Zhurnal Genet Selektsii
Vozilova AV, Tarasova AS, Ivanov EA, Pushkarev VP, Nalyotova NI, Pobedinskaya AI, Sabitova AS, Shilova NV.   +7 more
europepmc   +1 more source

Prokaryotic communities profiling of Indonesian hot springs using long-read Oxford Nanopore sequencing. [PDF]

BMC Res Notes
Wirajana IN, Ariantari NP, Shyu DJH, Vaghamshi N, Antaliya K, Dudhagara P.   +5 more
europepmc   +1 more source

Heparan sulfate in cerebrospinal fluid as a biomarker to assess disease severity and for treatment monitoring in patients with Mucopolysaccharidosis Type II: a position statement. [PDF]

Orphanet J Rare Dis
Giugliani R, de Siqueira ACM, Santos ES, Leão EKEA, Carvalho GDS, Santos MLSF, Raskin S, Martins AM.   +7 more
europepmc   +1 more source

Genetika frontotemporalnih demencija

Frontotemporalna demencija (FTD) je progresivni neurodegenerativni poremećaj koji prvenstveno zahvaća frontalne i temporalne režnjeve mozga dovodeći do značajnih promjena u osobnosti, ponašanju i govoru. To je drugi najčešći uzrok demencije s ranim početkom koji tipično pogađa osobe između 45. i 65. godine života. Etiologija FTD-a je vrlo heterogena, a
openaire   +1 more source

A familial case of interstitial deletion of the short arm of chromosome 6p22.3-p24.3 in twins with severe delay in psychomotor and speech development. [PDF]

Vavilovskii Zhurnal Genet Selektsii
Moskvitin GD, Kochkina DB, Gurinova MK, Fedotov DA, Bekenieva LV, Kashevarova AA, Sukhomyasova AL, Lebedev IN, Maximova NR.   +8 more
europepmc   +1 more source

Detection of Major Mutations in <i>CFTR, SERPINA1, HFE</i> Genes in Benign Unconjugated Hyperbilirubinemia Phenotype. [PDF]

Sovrem Tekhnologii Med
Ivanova AA, Apartseva NE, Kashirina AP, Nemtsova EG, Ivanova YV, Kruchinina MV, Kurilovich SA, Maksimov VN.   +7 more
europepmc   +1 more source